CN101578707B - Reel-to-reel reaction of precursor film to form solar cell absorber - Google Patents
Reel-to-reel reaction of precursor film to form solar cell absorber Download PDFInfo
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- CN101578707B CN101578707B CN2007800464593A CN200780046459A CN101578707B CN 101578707 B CN101578707 B CN 101578707B CN 2007800464593 A CN2007800464593 A CN 2007800464593A CN 200780046459 A CN200780046459 A CN 200780046459A CN 101578707 B CN101578707 B CN 101578707B
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- 239000010949 copper Substances 0.000 claims description 73
- 229910052738 indium Inorganic materials 0.000 claims description 58
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- 229910052711 selenium Inorganic materials 0.000 claims description 51
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- 239000002250 absorbent Substances 0.000 description 2
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- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910052581 Si3N4 Inorganic materials 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 description 1
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- JGIATAMCQXIDNZ-UHFFFAOYSA-N calcium sulfide Chemical compound [Ca]=S JGIATAMCQXIDNZ-UHFFFAOYSA-N 0.000 description 1
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- 229910000058 selane Inorganic materials 0.000 description 1
- IRPLSAGFWHCJIQ-UHFFFAOYSA-N selanylidenecopper Chemical compound [Se]=[Cu] IRPLSAGFWHCJIQ-UHFFFAOYSA-N 0.000 description 1
- VIDTVPHHDGRGAF-UHFFFAOYSA-N selenium sulfide Chemical class [Se]=S VIDTVPHHDGRGAF-UHFFFAOYSA-N 0.000 description 1
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- 229910010271 silicon carbide Inorganic materials 0.000 description 1
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- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
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- 229910052715 tantalum Inorganic materials 0.000 description 1
- MZLGASXMSKOWSE-UHFFFAOYSA-N tantalum nitride Chemical compound [Ta]#N MZLGASXMSKOWSE-UHFFFAOYSA-N 0.000 description 1
- 229910001936 tantalum oxide Inorganic materials 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- MTPVUVINMAGMJL-UHFFFAOYSA-N trimethyl(1,1,2,2,2-pentafluoroethyl)silane Chemical compound C[Si](C)(C)C(F)(F)C(F)(F)F MTPVUVINMAGMJL-UHFFFAOYSA-N 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
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- -1 tungsten nitride Chemical class 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/67—Apparatus specially adapted for handling semiconductor or electric solid state devices during manufacture or treatment thereof; Apparatus specially adapted for handling wafers during manufacture or treatment of semiconductor or electric solid state devices or components ; Apparatus not specifically provided for elsewhere
- H01L21/67005—Apparatus not specifically provided for elsewhere
- H01L21/67011—Apparatus for manufacture or treatment
- H01L21/67098—Apparatus for thermal treatment
- H01L21/67109—Apparatus for thermal treatment mainly by convection
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/18—Processes or apparatus specially adapted for the manufacture or treatment of these devices or of parts thereof
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/0248—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof characterised by their semiconductor bodies
- H01L31/0256—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof characterised by their semiconductor bodies characterised by the material
- H01L31/0264—Inorganic materials
- H01L31/032—Inorganic materials including, apart from doping materials or other impurities, only compounds not provided for in groups H01L31/0272 - H01L31/0312
- H01L31/0322—Inorganic materials including, apart from doping materials or other impurities, only compounds not provided for in groups H01L31/0272 - H01L31/0312 comprising only AIBIIICVI chalcopyrite compounds, e.g. Cu In Se2, Cu Ga Se2, Cu In Ga Se2
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/0248—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof characterised by their semiconductor bodies
- H01L31/0256—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof characterised by their semiconductor bodies characterised by the material
- H01L31/0264—Inorganic materials
- H01L31/032—Inorganic materials including, apart from doping materials or other impurities, only compounds not provided for in groups H01L31/0272 - H01L31/0312
- H01L31/0324—Inorganic materials including, apart from doping materials or other impurities, only compounds not provided for in groups H01L31/0272 - H01L31/0312 comprising only AIVBVI or AIIBIVCVI chalcogenide compounds, e.g. Pb Sn Te
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- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/04—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/18—Processes or apparatus specially adapted for the manufacture or treatment of these devices or of parts thereof
- H01L31/184—Processes or apparatus specially adapted for the manufacture or treatment of these devices or of parts thereof the active layers comprising only AIIIBV compounds, e.g. GaAs, InP
- H01L31/1844—Processes or apparatus specially adapted for the manufacture or treatment of these devices or of parts thereof the active layers comprising only AIIIBV compounds, e.g. GaAs, InP comprising ternary or quaternary compounds, e.g. Ga Al As, In Ga As P
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/541—CuInSe2 material PV cells
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/544—Solar cells from Group III-V materials
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Abstract
A roll-to-roll rapid thermal processing (RTP) tool with multiple chambers for forming a solar cell absorber by reacting a precursor layer on a continuous flexible workpiece. The RTP tool includes an elongated housing having a heating chamber with a predetermined temperature profile, a supply chamber and a receiving chamber. The heating chamber includes a small process gap in which the precursor layer is reacted with a Group VIA material to form an absorber layer. The continuous flexible workpiece is unrolled and advanced from the supply chamber into the heating chamber, and the processed continuous flexible workpiece is taken up and rolled in the receiving chamber.
Description
The cross-application of related application
The application is the part continuation application of No. the 11/549th, 590, the U.S. Patent application submitted on October 13rd, 2006.This application also requires to submit on November 10th, 2006 priority of No. the 60/865th, 385, U.S. Provisional Patent Application.At this these applications all are incorporated herein by reference.
Technical field
The present invention relates to be used for the preparation method and the device of film of the semiconductor film of radiation detector and photovoltaic applications occasion.
Background technology
Solar cell is the optoelectronic device that sunlight is directly changed into electric energy.Modal solar cell material is the silicon of monocrystalline or polycrystalline wafer form.Yet the cost of the electricity that the use silica-based solar cell produces is higher than the cost of the electricity that adopts the more conventional approach generation.Therefore, from nineteen seventies early stage since, people have made great efforts to reduce the cost of solar cell in order to use on earth.An approach that reduces the solar cell cost is the developing low-cost film growth techniques---its can be on large-area substrate the absorbent material of depositing solar cell quality, and use high production, cost effective method to make these equipment.
Comprise periodic table IB (Cu, Ag, Au) family, IIIA (B, Al, Ga, In, Ti) family and VIA family (O, S, Se, Te, Po) some IBIIIAVIA compound semiconductor of certain in material or the element is the splendid absorbent material that is used for film solar battery structure.Especially, the compound of Cu, In, Ga, Se and S (its be commonly referred to CIGS (S) or Cu (In, Ga) (S, Se)
2Or CuIn
1-xGa
x(S
ySe
1-y)
k, 0≤x≤1,0≤y≤1 wherein, and k is substantially equal to 2) be used in the solar battery structure near 20% conversion efficiency.The absorber that contains IIIA element al and/or the element T e of VIA family also is possible.Therefore, generally speaking, containing i) Cu of IB family, ii) at least a compound among S at least a and iii) VIA family, Se and the Te among In, Ga and the Al of IIIA family is applicable to solar cell application.
Shown in Fig. 1 such as Cu (In, Ga, Al) (S, Se, Te)
2The structure of the conventional IBIIIAVIA compounds of group photoelectric cell of thin-film solar cells.Device 10 is manufactured on the substrate 11, and substrate 11 is such as being sheet glass, sheet metal, insulation paillon foil or width of cloth material or conductive foil or width of cloth material.Comprise Cu (In, Ga, Al) (S, Se, Te)
2The absorber film 12 of material is grown on the conductive layer 13 in the family, and conductive layer 13 is deposited on the substrate 11 in advance and is used as the electrical contacts to this device.Substrate 11 forms base portion 20 with conductive layer 13.The conductive layer that comprises Mo, Ta, W, Ti and stainless steel etc. has been used in the solar battery structure of Fig. 1.If substrate self is the electric conducting material of suitably selecting, can not use conductive layer 13, because substrate 11 can be with the ohmic contact portion that connects this device.After the absorber film 12 of growing, be formed on the absorber film such as the hyaline layer 14 of CdS, ZnO or CdS/ZnO lamination.Ray 15 gets into this device through hyaline layer 14.The metal grill (not shown) also can be deposited on the hyaline layer 14 to reduce the effective series resistance of device.The preferred electric type of absorber film 12 is p types, and the preferred electric type of hyaline layer 14 is n types.Yet also can adopt n type absorber and p type Window layer.The preferred embodiment structure of Fig. 1 is called " substrate-type " structure.Also can form " coating " structure through following manner: with transparent conductive layer deposition on transparent coating such as glass or transparent polymer film, deposit then Cu (In, Ga, Al) (S, Se, Te)
2Absorber film finally forms the ohmic contact portion that is connected to this device by conductive layer.In this kind coat structure, light gets into said device from transparent coating side.Various materials through the whole bag of tricks deposition can be used in each layer that installs shown in Fig. 1 is provided.
In the thin-film solar cells that adopts IBIIIAVIA compounds of group absorber, battery efficiency becomes the majorant relation with the mol ratio of IB/IIIA.If in composition, contain more than one IIIA family material, the relative quantity of these IIIA elements or mol ratio also influence performance.For example, for Cu (In, Ga) (S, Se)
2Absorber layers, the efficient of device are the functions of Cu/ (In+Ga).Further, some important parameter of battery, such as its open circuit voltage, short circuit current and fill factor mol ratio along with the IIIA element---be that Ga/ (Ga+In) mol ratio changes.Usually, for good device performance, Cu/ (In+Ga) mol ratio remains on about 1.0 or be lower than 1.0.Along with Cu/ (In+Ga) mol ratio increases, on the other hand, the optical band gap of absorber layers increases, so the increase of the open circuit voltage of solar cell, and short circuit current can reduce usually.For film deposition process, importantly, can control the mol ratio of IB/IIIA in the component and the mol ratio of IIIA family composition.Should be noted that, although chemical formula often write as Cu (In, Ga) (S, Se)
2, this compound more the exact chemical formula be Cu (In, Ga) (S, Se)
k, wherein k is usually near 2 but can not be to be 2 just.In order to oversimplify, we are with continuing to be used for 2 k value.Need be pointed out that further that the symbol in the chemical formula " Cu (X, Y) " means X and all chemical compositions of Y from (X=0% and Y=100%) to (X=100% and Y=0%).For example " Cu (In, Ga) " means all chemical compositions from CuIn to CuGa.Similarly, Cu (In, and Ga) (S, Se)
2Mean the entire compound family that Ga/ (Ga+In) mol ratio from 0 to 1 changes and Se/ (Se+S) mol ratio from 0 to 1 changes.
Be used for growth for solar battery use used Cu (In, Ga) (S, Se)
2A kind of technology of type compound film is two phase process, wherein, Cu (In, and Ga) (S, Se)
2The metal ingredient of material at first deposits on the substrate, in The high temperature anneal, reacts with S and/or Se then.For example, for CuInSe
2Growth, Cu and In thin layer are deposited on earlier on the substrate, and this lamination precursor layer is reacted with Se at elevated temperatures then.If reaction environment also contains sulphur, and the CuIn that then can grow (S, Se)
2Layer.In said precursor layer, add Ga, just use Cu/In/Ga stack membrane predecessor, the Cu that allows to grow (In, and Ga) (S, Se)
2Absorber.
Two phase process schemes can also adopt the lamination that comprises VIA family material.For example, can through be deposited upon In-Ga-Se and Cu-Se in the In-Ga-Se/Cu-Se lamination and make they exist under the situation of Se reaction obtain Cu (In, Ga) (S, Se)
2Film.Similarly, also can use the lamination that comprises VIA family material and metal ingredient.The lamination that comprises VIA family material includes, but are not limited to In-Ga-Se/Cu lamination, Cu/In/Ga/Se lamination, Cu/Se/In/Ga/Se lamination etc.
Comprise selenizing and sulfuration or the vulcanization reaction of the precursor layer of metal ingredient can be various forms of VIA family material carry out.The gas that a kind of scheme relates to use such as H2Se, H2S or their mixtures simultaneously or in a sequence reacts, and predecessor comprises Cu, In and/or Ga.In this way, form after annealing that can be at high temperature and the reaction Cu (In, Ga) (S, Se)
2Film.Through during the process that forms at compound in reacting gas activated plasma, can increase reaction rate or respond.Se steam or S steam from element source also can be used for selenizing or sulfuration.Alternatively; As stated, Se and/or S can be deposited on the precursor layer that comprises Cu, In and/or Ga, and laminated construction can anneal at elevated temperatures with start metallic element or compound between VIA family material reaction and form Cu (In; Ga) (S, Se)
2Compound.
The reactions step of two phase process is carried out in batch furnace usually.In this scheme, the precut substrate that deposits precursor layer on several its is placed in the batch furnace, and 15 minutes to several hours time durations is carried out in reaction.After loading said substrate, the temperature of batch furnace is increased to reaction temperature usually, and reaction temperature can be in 400-600 ℃ scope.The slope that this temperature raises is usually less than 5 ℃/second, typically is lower than 1 ℃/second.The art methods of in No. the 5578503rd, United States Patent (USP), describing adopt rapid thermal annealing (RTP) scheme make precursor layer with batch mode react each substrate.In this kind design, the substrate temperature that has precursor layer is with high speed, and---being generally 10 ℃/second---is increased to reaction temperature.
The design that is used to carry out the reaction chamber of selenizing/vulcanizing treatment is extremely important for the quality of the compound film that obtains, efficient, output, material use and the processing cost of solar cell.The present invention provides method and apparatus to roll up the reaction of carrying out the precursor layer that is used to form CIGS (S) type absorber to the volume mode.Reel-to-reel or volume to volume are handled to be increased output and makes substrate processing minimize.Therefore, it is the method for optimizing that is used to produce in enormous quantities.
Summary of the invention
The present invention provides the instrument of a kind of method and a kind of integrated form on the continuous flexible workpiece, to form solar cell absorber.The volume that use comprises a plurality of chambeies makes the precursor layer reaction on the continuous flexible workpiece to rolling up rapid thermal treatment (RTP) instrument.
One aspect of the present invention provides a kind of integrated form volume with a plurality of chambeies to come through making the precursor layer reaction on the continuous flexible surface of the work form solar cell absorber to rolling up the RTP instrument.Said instrument comprises: long and narrow housing, it comprises vacuum pipeline and in said long and narrow housing, vacuumizes.Further, the heating chamber of said long and narrow housing is applied to said continuous flexible workpiece with predefined Temperature Distribution.Said heating chamber is at first opening at the said heating chamber first end place with between second opening at the said heating chamber second end place, extend, and comprises the processing gap that roof, diapire and sidewall limited said heating chamber.The gas access pipeline that closes on the first opening setting of said heating chamber can be that inert gas can comprise that maybe the processing gas of VIA family material is sent in the said heating chamber during said processing.Said continuous flexible workpiece setting becomes during handling, to pass through said processing gap and between said first and second openings, is transmitted.Depend on the Temperature Distribution that preestablishes of speed and the heating chamber of flexible workpiece in handling the gap, the part of said flexible workpiece during reaction stands predefined temperature-time curve.
The supply chamber of said long and narrow housing holds the feed rolls of said continuous flexible workpiece.First end and said first opening that said heating chamber is closed in said supply chamber is connected to said processing gap with the inner space in said supply chamber, and said continuous flexible workpiece setting becomes through said first opening and is transferred into said heating chamber from said supply chamber.The reception cavity of said long and narrow housing holds the continuous flexible workpiece from said heating chamber.Said second opening is connected to the processing gap with the inner space of reception cavity, and said continuous flexible workpiece setting becomes said second opening of process to be transferred into said supply chamber from said process chamber.
Part through unwinding in advance on the said feed rolls from said supply chamber of the said continuous flexible workpiece of feeding; And through in reception cavity, picking up and the processing section of the said continuous flexible workpiece of reeling, travel mechanism keeps in the processing gap of said heating chamber and moves said continuous flexible workpiece (part that is in the process chamber and in process chamber, has handled that comprises said continuous flexible workpiece) and make it to pass through said processing gap.
The discharge pipe that one of first and second openings that close on said heating chamber are provided with is removed and is handled gas and gaseous by-product.Gas inlet pipe line and discharge pipe are arranged to: when the continuous flexible workpiece moves in the processing gap, exist on the front surface of permission continuous flexible workpiece and handle gas stream.
Description of drawings
Fig. 1 is the cutaway view that adopts the solar cell of IBIIIAVIA family absorber layers.
Fig. 2 illustrates with the volume to volume mode and makes the precursor layer reaction on the flexible membrane matrix, to form the device of IBIIIAVIA family layer.
Fig. 3 A illustrates the exemplary flexible structure that comprises flexible substrate and deposition precursor layer above that.
Fig. 3 B illustrates a matrix, and this matrix has the formed IBIIIAVIA family absorber layers through the precursor layer reaction that makes Fig. 3 A above that.
Fig. 4 illustrates another makes the precursor layer reaction on the flexible membrane matrix, to form the device of IBIIIAVIA family layer with the volume to volume mode.
Fig. 5 A-5B illustrates the cutaway view in the differential responses chamber that flexible structure is set in it.
Fig. 5 C illustrates the cutaway view of the reaction chamber that comprises exocoel and inner chamber.
Fig. 6 illustrates the example of the reactor of Fig. 2.
Embodiment
Comprise that IB family material, IIIA family material and optional VIA family material or the predecessor of component and the reaction of VIA family material can obtain in many ways.These technology relate under the situation at least a in having Se, S and Te the temperature that precursor layer is heated to 350-600 ℃; Preferably be heated to 400-575 ℃ temperature; And continuing period from 1 minute to several hours, wherein said Se, S and/or Te are by providing such as following source: i) directly be deposited on solid-state Se, S or Te source on the said predecessor; And ii) H
2Se gas, H
2S gas, H
2Te gas, Se steam, S steam, Te steam etc.Se, S, Te steam also can produce through the solid source of heating away from these materials of predecessor.Such as H
2Se and H
2The hydride gas of S can be bottled gas.This kind hydride gas and such as H
2The short life gas of Te also can produce at the scene, for example, through electrolysis in comprising the negative electrode acidic aqueous solution of S, Se and/or Te, provides to reactor then.The electrochemical method of producing these hydride gas is applicable to produced on-site.
Predecessor can be side by side or sequentially is exposed to more than one VIA family material.For example, comprise Cu, In, Ga and Se precursor layer can exist under the situation of S annealing with form Cu (In, Ga) (S, Se)
2In the case, precursor layer can be to comprise metal level that contains Cu, Ga and In and the layer that piles up that is deposited on the Se layer on the metal level.Alternatively, the Se nano particle can spread all in the metal level that is dispersed in the said Cu of containing, Ga and In.Said precursor layer can also comprise Cu, In, Ga and S, during reaction this layer exist under the situation of Se annealing with form Cu (In, Ga) (S, Se)
2
Formation Cu (In, and Ga) (S, Se)
2Some preferred implementations of compound layer can be summed up as follows: i) Se is deposited upon on the metal precursor that comprises Cu, In and Ga and forms a structure and said structure is reacted in gaseous state S source; Ii) mixed layer or S layer and the Se layer of deposition S and Se on the metal precursor that comprises Cu, In and Ga form a structure and also make said structure in the gaseous environment that does not contain S or Se or containing in the gaseous environment at least a among S and the Se and react at elevated temperatures; Iii) deposition S layer on the metal precursor that comprises Cu, In and Ga forms a structure and said structure is reacted in gaseous state Se source; Iv) deposition Se layer forms a structure on the metal precursor that comprises Cu, In and Ga, and makes said structural response to form Cu (In, Ga) Se at elevated temperatures
2Layer and/or the mixing that comprises Cu, In and Ga selenides mutually layer make said Cu (In, Ga) Se then
2Layer and/or said mixes mutually layer and gaseous state S source, liquid S source or reacts such as the solid-state S source of S layer; V) deposition S layer forms a structure on the metal precursor that comprises Cu, In and Ga, and makes said structural response to form Cu (In, Ga) S at elevated temperatures
2Layer and/or the mixing that comprises Cu, In and Ga selenides mutually layer make said Cu (In, Ga) S then
2Layer and/or said mixes mutually layer and gaseous state Se source, liquid Se source or reacts such as the solid-state Se source of Se layer.
Should be noted that VIA family material is corrosive.Therefore, being exposed to the reactor of VIA family material or material steam or the used material of each several part in chamber at elevated temperatures should correctly select.These parts should be with following material manufacture or coating: such as the pottery material of inertia in fact such as aluminium oxide, tantalum oxide, titanium oxide, zirconia etc., glass, quartz, stainless steel, graphite for example; Such as the heat proof material of Ta, such as tantalum nitride and/ramet, titanium nitride and or the heating resisting metal nitride and/or the carbide of titanium carbide, tungsten nitride and/or tungsten carbide; And such as silicon nitride with or other nitride and/or the carbide of carborundum etc.
The reaction that comprises the precursor layer of Cu, In, Ga and at least a alternatively VIA family material can be carried out in the reactor that treatment temperature is applied to said precursor layer with slow speed.Alternatively, can use rapid thermal treatment (RTP), wherein with about at least 10 ℃/second speed with the predecessor temperature paramount reaction temperature that raises.If include VIA family material in the precursor layer, then VIA family material can obtain through evaporation, splash or plating.Alternatively, can prepare the ink that comprises VIA family nanoparticle, these inks can deposit and in precursor layer, form VIA family material layer.Can also use other liquid or solution such as the organic metal solution that comprises at least a VIA family material.Can adopt and immerse in deposite metal or the ink, spray the deposite metal or ink, wiper or the ink technology of writing deposit this kind layer.
The reaction that is used for carrying out precursor layer shown in Fig. 2 with the volume to volume device 100 that forms IBIIIAVIA compounds of group film or volume to rolling up the RTP reactor.Should be noted that and treat that the precursor layer of in this reactor, reacting can comprise at least a IB family's material and at least a IIIA family material.For example; Precursor layer can be the lamination of Cu/In/Ga, Cu-Ga/In, Cu-In/Ga, Cu/In-Ga, Cu-Ga/Cu-In, Cu-Ga/Cu-In/Ga, Cu/Cu-In/Ga or Cu-Ga/In/In-Ga etc., and the order of wherein various material layers in said lamination can change.At this, Cu-Ga, Cu-In, In-Ga mean alloy or the alloy of mixture, Cu and In or alloy or the mixture of mixture and In and Ga of Cu and Ga respectively.Alternatively, precursor layer can also comprise at least a VIA family material.This kind precursor layer has many examples.In these examples some are Cu/In/Ga/VIA family material laminate, Cu-VIA family material/In/Ga lamination; In-VIA family material/Cu-VIA family material laminate or the material/Cu/In of Ga-VIA family; Alloy, mixture or the compound (such as copper selenide, copper sulfide etc.) that comprise Cu and VIA family material at this Cu-VIA family material; In-VIA family material comprises alloy, mixture or the compound (such as indium selenide, indium sulfide etc.) of In and VIA family material, and Ga-VIA family material comprises alloy, mixture or the compound (such as calcium selenide, calcium sulfide etc.) of Ga and VIA family material.These predecessors are deposited on the matrix 20 that comprises substrate 11, and matrix 20 can additionally comprise conducting shell as shown in fig. 1 13.Other type predecessor that can use method and apparatus of the present invention to handle comprises IBIIIAVIA family material layer, this IBIIIAVIA family material layer can use such as compound plating, chemical plating, from the splash of compound target, adopt deposit of ink, splash based on the ink of IIIAVIA family nanoparticle comprise Cu, In, Ga and alternatively Se etc. low temperature method such as metallic nano-particle and be formed on the matrix.These material layers are annealed in said device or reactor in 350-600 ℃ temperature range then, to improve its crystal mass, component and density.
Annealing and/or reactions step can be in reactor of the present invention be carried out with the pressure that is substantially equal to atmospheric pressure, the pressure that is lower than the pressure of atmospheric pressure or is higher than atmospheric pressure.Lower pressure in the reactor can obtain through using vacuum pump.
The volume to volume device 100 of Fig. 2 can comprise elongated heating chamber 101, and heating chamber 101 can be had such as one or more thermals treatment zone of Z1, Z2 and Z3 to form along the chamber Temperature Distribution of 101 length around, heater system 102 by heater system 102.Between said district, be provided preferably with the buffer area of lower thermal conductivity, the feasible Temperature Distribution that can obtain drastic change.That the details of this of buffer area kind of use was submitted on October 13rd, 2006, denomination of invention had discussion in No. the 11/549/590th, the U.S. Patent application of " Method and Apparatus for Converting Precursor Layers intoPhotovoltaic Absorbers ", at this this U.S. Patent application was incorporated herein by reference.Chamber 101 integral body are attached to first port one 03 and second port one 04 with sealable mode.Internal capacity, first port and second port that " integrally with sealable mode " means the chamber seal with respect to air ambient; Therefore; Any gas that in internal capacity, uses can not let out (except the discharge port in appointment), and does not have escape of air among internal capacity.In other words, the integrated of said chamber, first and second ports is vacuum-packed.The first reel 105A and the second reel 105B are separately positioned in first port one 03 and second port one 04; The continuous flexible workpiece 106 of flexible structure can move with arbitrary direction between the first reel 105A and the second reel 105B, from left to right or from right to left promptly.Flexible structure comprises the precursor layer of treating in elongate chamber, to be converted into absorber layers.First port one 03 has at least one the first port gas access 107A and the first port vacuum pipeline 108A.Similarly, second port one 04 has at least one second port gas access 107B, and can have the second port vacuum pipeline 108B.The elongated heating chamber 101 and first port one 03 and second port one 04 can be through any one or two and the emptyings among the first port vacuum pipeline 108A and the second port vacuum pipeline 108B.Chamber 101 also is provided with at least one gas line 113 and at least one discharge portion 112.Can there be additional vacuum pipeline (not shown) to be connected to chamber 101.Preferably, valve 109 is set on all gas inlet, gas line, vacuum pipeline and outlet, makes to form a common cavity, this common cavity can be under the single vacuum.101 two ends preferably have otch 110 in the chamber, and flexible structure 106 is passed said otch.Although with chamber and first and second evacuation port is to remove the method for optimizing of air from the internal capacity of this instrument, utilize such as N
2The discharge port of gas through appointment the internal capacity of this instrument purged also be fine.
Embodiment 1
Can use single chamber reactor of Fig. 2 to design to form Cu (In, Ga) (Se, S)
2Absorber layers.Flexible structure 106A before the reaction of example has been shown in Fig. 3 A.Matrix 20 can be similar to the matrix 20 of Fig. 1.Precursor layer 200 is arranged on the matrix 20.Precursor layer 200 comprises Cu, and comprises at least a among In and the Ga.Preferably, precursor layer 200 comprises each among Cu, In and the Ga.Alternatively, Se layer 201 can be deposited on and form the precursor layer 202 of carrying Se on the precursor layer 200.Se can also be blended in another form that forms the precursor layer of carrying Se in precursor layer 200 (not shown).Flexible structure after the reactions step is shown in Fig. 3 B.In the case, flexible structure 106B comprises matrix 20 and IBIIIAVIA compound layer 203---such as through precursor layer 200 or carry the Cu that the reaction of the precursor layer 202 of Se obtains (In, Ga) (Se, S)
2Film.
After on unreacted flexible structure 106A or width of cloth material being carried in for example the first reel 105A, an end of said width of cloth material can be fed through chamber 101, and the gap 111 through otch 110 twists on the second reel 105B then.The door (not shown) of first port one 03 and second port one 04 is closed, and said system (comprising first port one 03, second port one 04 and chamber 101) is drained to remove air.Alternatively, can utilize through in said gas access or the gas line any or all get into and said system being purged through outlet 112 of lasting a period of time such as the inert gas of N2.After emptying or purging, system be filled with inert gas and heater system 102 can open with along the chamber 101 length set up Temperature Distribution.When setting up required Temperature Distribution, reactor can be prepared to be used for to handle.
Forming for example Cu (In, Ga) Se
2In the processing of absorber layers, comprise the Se steam or such as H
2The gas in the Se source of Se can be imported in the chamber, preferably imports through gas access, chamber 113.Outlet can be opened through opening its valve now, makes the gas that carries Se can be directed to washer or trap (not shown).Should be noted that Se is that near volatile material and about 400-600 ℃ typical reaction temperature, being tending towards is attached on any cold surface and with the form deposition of solid-state or liquid Se.This means; Only if during reaction treatment, take precautions against, otherwise the Se steam can get into first port one 03 and/or second port one 04 and be deposited on all surface (comprising the non-reacted parts of the width of cloth material in first port one 03 and the reactive moieties of the width of cloth material in second port one 04).In order to eliminate this kind Se deposition or to make it to minimize, preferably gas is imported in first port one 03 and through the second port gas access 107B gas is imported second port one 04 through the first port gas access 107A.The gas that is imported into can be the gas that can not resolve into the carrying Se of Se and/or S at low temperatures and/or carry S, but the preferably said gas that is imported into is such as N
2Inert gas, and said inert gas to said two ports pressurization to set up inert gas flow from the gap 111 of said port through said otch 110 towards said chamber.
The speed of this gas flow can increase through gap 111 that reduces otch 110 and/or the flow that increases in gas to the said port.Under this mode, the diffusion of Se steam to said port is reduced or prevents, this kind steam is guided to outlet 112, is collected away from the width of cloth material of having handled this its.Gap 111 preferred values for otch 110 can be in the scope of 0.5-5mm, more preferably in the scope of 1-3mm.Gas flows into the flow of said port can be according to the width of otch and adjusted, and the width of said otch depends on the width of flexible structure 106 or width of cloth material.Usually width of cloth material width can be in the scope of 1-4 foot.
In case carry the gas of Se or the temperature required distribution that inert gas flow was set and had reached chamber 101, the speed that flexible structure 106 can be scheduled to moves to second port one 04 from first port one 03.In this way, the non-reacted parts of flexible structure 106 is left the first cylinder 105A, gets into chamber 101, through chamber 101, accomplishes reaction and on the matrix of width of cloth material, forms Cu (In, Ga) Se
2Absorber layers, and in second port one 04, twist on the second reel 105B.Should be noted that in second port one 04, can have optional cooled region (not shown) to be rolled onto on the second reel 105B with the width of cloth material that was reacting cools off it before.
Top explanation also can be used to form the absorber layers that contains S.For example, in order to form Cu (In, Ga) S
2Layer, the gas of the carrying Se in the explanation can be by such as H above
2The gas instead of the carrying S of S.For form Cu (In, Ga) (Se, S)
2Layer can use gas that carries Se and the mixture that carries the gas of S.Alternatively, can use the predecessor and the reaction of carrying S in the gas that carries S, to carry out.
A characteristic of the system 100 of Fig. 2 is that flexible structure 106 can move also from left to right and can move from right to left.In this way, can carry out reactions step more than once.For example, can move and carry out first reaction from left to right, can react along with width of cloth material moves second from right to left then, and reacted width of cloth material can unload from the first reel 105A along with width of cloth material.Certainly, can through between the first reel 105A and the second reel 105B repeatedly moving web carry out reaction or annealing of a plurality of steps etc.For different reactions step, can be different such as the reaction condition of gas flow and reaction temperature.For example, when width of cloth material moved from left to right, for first reactions step, the Temperature Distribution in chamber 101 can be set to 400 ℃ of maximum temperatures.The predecessor of width of cloth material can be 400 ℃ ground, temperature lower part or reaction fully or annealing in this way.
After roughly all parts of width of cloth material twist on the second reel 105B; The maximum temperature of Temperature Distribution can be adjusted to higher value; Such as being adjusted to 550 ℃; This moment, said width of cloth material can move from right to left under 550 ℃ of higher temperature, had annealed or the precursor layer of reacting can be reacted further, annealing or crystalization.Should be noted that and can realize similarly handling through following method: make chamber 101 longer, and 101 Temperature Distribution is set, make along with width of cloth material moves from left to right along the chamber, for example through 400 ℃ zone, and then through 550 ℃ zone.Yet, use aforesaid bidirectional-movement, the length in chamber 101 can reduce and still can realize the reaction of two step/two temperature.To keep width of cloth material to have high temperature in order between reactions step, being rolled onto on the first reel 105A or the second reel 105B arbitrary one at width of cloth material, can optional heater (not shown) to be set within one or two the arbitrary of first port one 03 and second port one 04.
Should be noted that the reacting gas composition also can change in the rapid reaction method of above-mentioned multistep outside temperature of reactor and width of cloth material speed.For example, during first reactions step, when width of cloth material moves from left to right, such as H
2First gas of Se can be used in the chamber 101 to form the precursor layer of selenizing.On the other hand, during second reactions step, when width of cloth material moves from right to left, such as H
2Another gas of S can be imported in the chamber 101.As a result, along with width of cloth material moves to the first reel 105A from the second reel 105B, the precursor layer of selenizing can be reacted with S, thus through the precursor layer with selenizing change into sulphur-selenides can grow Cu (In, Ga) (Se, S)
2Layer.Select gas concentration, width of cloth material speed and reaction temperature, can control the amount of Se and S in the absorber layers.For example, when the reaction of carrying out with Se,, can increase S/ (Se+S) molar ratio in the final absorber layers through increasing the width of cloth material speed during first treatment step and/or reducing reaction temperature.Similarly, when the reaction of carrying out with S,, also can increase S/ (Se+S) molar ratio through reducing width of cloth material speed and/or the rising reaction temperature during second reactions step.This provides through optimizing two reactions step independent of each other optimizes the big flexibility of absorber layers composition.
Another embodiment of the present invention is shown in Fig. 4.Reactor assembly 400 among Fig. 4 comprises syllogic chamber 450---it is the example of multi-cavity design more generally.The syllogic chamber 450 of Fig. 4 comprises A section, B section and C section.Heater and first port, first reel, second port and second reel around each section is not shown in the drawings to simplify this figure.But, can be used for the part that these do not show with similar design shown in Fig. 2.Said heater can be heating lamp, heat coil etc., and they can have independently control to come in A section, B section and C section, to produce different temperature value and distribution.
The key character of the design of Fig. 4 is that the A section is separated by sections with the C section, is preferably separated by low volume segments 410, and low volume segments 410 is in the B section in syllogic chamber 450.There is device that gas is imported each section in A section, B section and the C section.For example, inlet 401 and 402 can import A section and C section with gas respectively, 403 can gas be imported the low volume segments 410 in the B section and enter the mouth.Outlet 404 and 405 can be set discharge gas from A section and C section respectively.Flexible structure 106 pending or reaction can get into syllogic chamber 450 through the first gap 111A of the first otch 110A, and the second gap 111B through the second otch 110B discharges then.
Embodiment 2
Can use the syllogic chamber of Fig. 4 form Cu (In, Ga) (Se, S)
2Absorber layers.After being written into unreacted flexible structure 106, as explanation among the embodiment 1, system is bled and purges, can begin to handle.The A section in syllogic chamber 450, B section and C section can have temperature T 1, T2 and T3, and T1, T2 and T3 can be same to each other or different to each other.Further, A section, B section and C section all can have Temperature Distribution separately, but not have stationary temperature along its length separately.During handling, can 403 will be such as N through inlet
2First handle gas and import the low volume segments 410 in the B section, and second handle gas and the 3rd and handle gas and can be respectively 401 and 402 be directed into A section and C section respectively through entering the mouth.
It can be same gas or two kinds of different gases that the second processing gas and the 3rd is handled gas.For example, second handles gas can comprise Se, and the 3rd processing gas can comprise S.In this way, when the part of the flexible structure 106 first gap 111A through the first otch 110A got into the A section in syllogic chamber, the precursor layer on this part began to be reflected at the precursor layer that forms selenizing on the said part with Se.When said part gets into low volume segments 410, its in this section at N
2Annealing (if the B section is heated) in the gas gets into the C section up to said part.In the C section, owing to have the S of gaseous form, thus sulfuration or vulcanization reaction take place, thereby before the second gap 111B discharge syllogic chamber 450 of said part through the second otch 110B, on said part, form Cu (In, and Ga) (Se, S)
2Absorber layers.Can control S/ (Se+S) molar ratio in the absorber layers through the relative temperature and the length of A section and C section.For example, under given width of cloth material speed, can increase S/ (Se+S) ratio through length that reduces the A section and/or the temperature that reduces the A section.
Alternatively or additionally, can increase the length and/or the temperature of C section.Can carry out opposite operation to reduce S/ (Se+S) molar ratio.Should be noted that as the same in last embodiment, can be from right to left to backhauling capable flexible structure to proceed reaction.The gas that can also change A section, B section and each section of C section of importing syllogic chamber 450 is to obtain to have the absorber layers of different component.The uniqueness of the design of Fig. 4 is characterised in that; Permission exists two kinds of different gases or steam in two of reactor different sections, making can be through applying different temperature and different reactive gas to each section of width of cloth material and on width of cloth material substrate, carrying out volume to volume and handle continuously in a sequential manner.The low volume segments that inert gas is imported between two sections (the A section among Fig. 4 and C sections) hinders as diffusion, and makes that the mutual mixing between the employed gas with various minimizes or eliminate this kind mixing each other in these two sections.First gas stream that imports through the inlet among Fig. 4 403 flow to the right and flows left through low volume segments 410, against towards each other any gas flow between A section and the C section.Should be noted that; In the reactor design of Fig. 4, can increase more section; So that have more low volume segments between section and the section, and each section can the gentle running body of different temperature, so that the processing flexibility of formation high-quality IBIIIAVIA compounds of group absorber layers to be provided.In addition, can more gas access and/or outlet be added into the system of Fig. 4, and the position of these gas accesses and outlet can change.
Various shape of cross section can be used for chamber of the present invention.Two kinds of such chamber 500A and 500B with circular and rectangular cross section are shown respectively in Fig. 5 A and 5B.General cylindrical shape reaction chamber with circular cross section is favourable in the chamber, vacuumizing, even also be like this in the chamber by such as glass or quartzy material manufacture the time.Yet along with the width of substrate or width of cloth material increases to 1 foot, 2 feet or bigger, it is quite big that circular cavity becomes.Use the big cylindrical chamber of this kind can not keep Temperature Distribution, thereby volume is handled and can not on such as 1-4 feet wide or wideer wide flexible substrate, be carried out to rolling up RTP with violent variations in temperature.
Shown in Fig. 5 B, chamber 500B comprises the rectangle gap that is limited roof 510A, diapire 510B and sidewall 510C.In the case, the chamber preferably is made up of metal, because do not break in the chamber in order in this kind chamber, to vacuumize, constitutes the then very thick wall (half inch or thicker) of needs like fruit caving by quartz or glass.In this structure, roof 510A and diapire 510B are parallel basically, and flexible structure 106 is arranged between them.Chamber with rectangular cross section or structure more helps reducing the consumption of reacting gas, is lower than 10mm because the height in this kind chamber can be reduced to, and width is near the width (can be the 1-4 foot) of flexible structure.So little height also allows under need not the situation in the too many VIA family material introduction chamber, in VIA family steam, to react.Should be noted that the height of chamber 500B, promptly gap size is the distance between roof and the diapire, and the gap size that needs to keep little is during reaction to keep high VIA family material pressure on the surface of precursor layer.In addition, even these chambeies also can keep the Temperature Distribution of acute variation in the flexible substrate more than 4 feet for width.For example, the Temperature Distribution along the length in the chamber with square-section can comprise 400-500 ℃ variations in temperature on several centimetres length.Therefore, this kind chamber can be used to rolling up in the RTP pattern at volume, and wherein through above-mentioned variations in temperature, the temperature that stands 400-500 ℃/second raises the part of the precursor layer on the substrate with the speed of several centimetres of per seconds.Through speed that increases substrate even the higher rate that can realize the thousands of degree of per second.
As shown in the cross-sectional view of Fig. 5 C, another preferred chamber design comprises dual chamber 500C, and the inner chamber 501B that wherein has the square-section is arranged in columnar, as the to have circular cross-section exocoel 501A.In the case, flexible structure 106 or width of cloth material are through inner chamber 501B, and inner chamber 501B can be square in shape, and all air-flows preferably are directed to and through inner chamber 501B, the volumetric ratio exocoel 501A of 501B is little a lot.Through this kind mode, the waste of reacting gas realizes minimizing, but meanwhile because the whole chamber of the cylindrical shape emptying easily of exocoel 501A, even said chamber can be such as the material manufacture of quartz.The heater (not shown) can be arranged on the outside of inner chamber 501B, the inboard of exocoel 501A in the case.In this way, the Temperature Distribution that can keep drastic change along the chamber, square-section has the ability of emptying reactor body portion easily simultaneously.
Fig. 6 illustrates the example of the reactor of Fig. 2.Only show cavity segment in order to simplify accompanying drawing.As finding out from this figure, dual chamber 600 comprises cylindrical chamber 601 and the rectangular cavity 602 that is placed in the cylindrical chamber 601.Gas access 113 is connected to rectangular cavity 602 with outlet 112.Should be noted that cylindrical chamber 601 can be not airtight with respect to rectangular cavity, thereby when whole chamber is evacuated, the pressure balance between cylindrical chamber 601 and the rectangular cavity.Otherwise if these chambeies are airtight each other, they must be evacuated so that there is not big pressure reduction between them simultaneously.
Can use material as known in the art and method to be to make solar cell on the formed compound layer in the reactor of the present invention.For example, can use (<0.1 micron) CdS layer of chemical impregnation method deposition of thin on said compound layer.Can use MOCVD or splash technology on said CdS layer, to deposit the transparency window of ZnO.Plated metal refers to that pattern is to accomplish solar cell on said ZnO alternatively.
Although describe the present invention in conjunction with some preferred implementation, mode for the person of ordinary skill of the art, its remodeling is tangible.
Claims (41)
1. the volume of an integrated form is to rolling up rapid thermal treatment (RTP) instrument, and it is used for forming solar cell absorber through the lip-deep precursor layer reaction that makes the continuous flexible sheet-like workpiece, and said instrument comprises:
Elongated housing, it comprises the common cavity of sealing, and said common cavity comprises heating chamber, supply chamber and reception cavity, wherein:
Said heating chamber comprises narrow processing gap; Said narrow processing gap is applied to being on the part in this narrow processing gap of said continuous flexible sheet-like workpiece with predefined Temperature Distribution; Wherein said narrow processing gap is limited the roof that forms opening, diapire and sidewall; The highly significant of wherein said opening is less than its width, and said narrow processing gap have feed opening, outlet opening and be arranged on said feed opening and said outlet opening between be used for discharge pipe that the gaseous state thing from the said narrow processing gap of said heating chamber is removed;
Said supply chamber holds the feed rolls of said continuous flexible sheet-like workpiece; And has supply chamber opening; Wherein, said supply chamber opening is aimed at the feed opening in said narrow processing gap, and said continuous flexible sheet-like workpiece is arranged to get into said heating chamber from said supply chamber;
Said reception cavity holds the reception roller to collect said continuous flexible sheet-like workpiece from said heating chamber; And has the reception cavity opening; Wherein, Said reception cavity opening is aimed at the outlet opening in said narrow processing gap, and said continuous flexible sheet-like workpiece is arranged to get into said reception cavity from said heating chamber; And
Travel mechanism; It keeps said continuous flexible sheet-like workpiece in said common cavity; And; Through the part of the unwinding in advance on said feed rolls of said continuous flexible sheet-like workpiece being sent to and processing section through picking up said continuous flexible sheet-like workpiece and it is wound on the reception roller the said reception cavity, move said continuous flexible sheet-like workpiece and make it said narrow processing gap through said heating chamber.
2. according to the instrument of claim 1, it is characterized in that, further comprise the vacuum pipeline that is associated with said common cavity, said vacuum pipeline allows in said common cavity inner formation vacuum and with the inner emptying of said common cavity.
3. according to the instrument of claim 2, it is characterized in that further comprise the cylindrical enclosure around said heating chamber, wherein said cylindrical enclosure is sealed to said thin-long casing.
4. according to the instrument of claim 1; It is characterized in that; The said narrow processing gap of said heating chamber is through being arranged on the external heated element heating in said narrow processing gap, thereby makes the roof, diapire and the sidewall that limit said processing gap be heated, and forms said Temperature Distribution.
5. according to the instrument of claim 4; It is characterized in that; Further comprise the gas inlet pipe line that the feed opening that closes on said narrow processing gap is provided with; The said narrow processing gap that it is configured to processing gas is imported said heating chamber makes said processing gas flow along the direction of motion of said continuous flexible sheet-like workpiece.
6. according to the described instrument of claim 5; It is characterized in that; Said supply chamber and said reception cavity include the gas access separately; Respectively inert gas is sent in said supply chamber and the said reception cavity; Thereby set up from said supply chamber the inert gas flow that feed opening through said narrow processing gap gets into said narrow processing gap, and get into the inert gas flow in said narrow processing gap, thereby prevent that the gaseous state thing in the said narrow processing gap from getting into said supply chamber and said reception cavity from the outlet opening of said reception cavity through said narrow processing gap.
7. according to the described instrument of claim 4, it is characterized in that the distance between said roof and the said diapire changes on the length in the said processing gap of said heating chamber.
8. according to the described instrument of claim 7, it is characterized in that the feed opening and the outlet opening in said narrow processing gap all comprise separator separately, said separator limits the gap less than said processing gap.
9. according to the instrument of claim 5, it is characterized in that said gas inlet pipe line is supplied to VIA family material processed gas in the said heating chamber.
10. according to the instrument of claim 4; It is characterized in that; The equal separately air inclusion inlet of said supply chamber and said reception cavity; Respectively inert gas is transferred in said supply chamber and the said reception cavity being used for; Thereby set up from said supply chamber the inert gas flow that feed opening through said narrow processing gap gets into said narrow processing gap, and get into the inert gas flow in said narrow processing gap, thereby prevent that the gaseous state thing in the said narrow processing gap from getting into said supply chamber and said reception cavity from the outlet opening of said reception cavity through said narrow processing gap.
11. the instrument according to claim 4 is characterized in that, the roof in said narrow processing gap is parallel to the diapire in said narrow processing gap in fact.
12. the instrument according to claim 11 is characterized in that, the height in said narrow processing gap is in the scope of 0.5-10mm.
13. the instrument according to claim 12 is characterized in that, the width in said narrow processing gap is in the scope of 100-2000mm.
14. a rapid thermal treatment (RTP) system, it is used for forming solar cell absorber through the precursor layer of deposition reaction in advance on the surface that makes the continuous flexible sheet-like workpiece, and said system comprises:
Heating chamber; It allows within it portion to form vacuum and with its inner emptying; Said heating chamber comprises first processing section, diffusion hinders the section and second processing section; Said heating chamber provides predetermined Temperature Distribution to the part that is sent to through said heating chamber of said continuous flexible sheet-like workpiece, wherein:
Said first processing section is through the part in said first processing section heats and handles to being in of said continuous flexible sheet-like workpiece under the situation about existing at least a first gaseous state thing, and said first processing section comprises the first narrow processing gap;
Said second processing section is through the part in said second processing section heats and handles to being in of said continuous flexible sheet-like workpiece under the situation about existing at least a second gaseous state thing, and said second processing section comprises the second narrow processing gap;
Wherein, the said first narrow processing gap and the said second narrow processing gap imposes on the continuous flexible sheet-like workpiece part that is arranged in it with the different piece of said predetermined temperature profile separately; And
The said first narrow processing gap and the said second narrow processing gap limits by the roof, diapire and the sidewall that form opening separately; The highly significant of wherein said opening is less than its width, and the said first narrow processing gap and the said second narrow processing gap all have feed opening, outlet opening and be arranged on said feed opening and said outlet opening between be used for discharge pipe that the gaseous state thing from the corresponding first narrow processing gap and the second narrow processing gap is removed;
Said diffusion hinders section and is arranged between the said first narrow processing gap and the second narrow processing gap; Through setting up from central area that said diffusion hinders section the inert gas flow in the narrow processing gap of outlet opening through the said first narrow processing gap hinders section towards the inert gas flow in the said first narrow processing gap and from said diffusion the central area feed opening court said second through the said second narrow processing gap; Form to hinder the mutual mixing that reduces said at least a first gaseous state thing and the said at least a second gaseous state thing thus, thereby the processing in the said first narrow processing gap and the second narrow processing gap is separated; And
Travel mechanism; It is fed to said heating chamber through the part with the unwinding in advance on the feed rolls of said continuous flexible sheet-like workpiece; And the processing section through picking up said continuous flexible sheet-like workpiece and it is wound on receives on the roller, thereby within each section of said heating chamber, keeps and move said continuous flexible sheet-like workpiece making it through each section.
15. the system according to claim 14 is characterized in that, further comprises the supply chamber to hold the feed rolls of said continuous flexible sheet-like workpiece, wherein said supply chamber and said heating chamber become one.
16. the system according to claim 15 is characterized in that, further comprises reception cavity to hold the reception roller of said continuous flexible sheet-like workpiece, wherein said reception cavity and said heating chamber become one.
17. system according to claim 16; It is characterized in that; The equal separately air inclusion inlet of said supply chamber and said reception cavity; Respectively inert gas is transferred in said supply chamber and the said reception cavity being used for; Thereby set up from said supply chamber the inert gas flow that feed opening through the said first narrow processing gap gets into the said first narrow processing gap, and get into the inert gas flow in the said second narrow processing gap, thereby prevent that the gaseous state thing in the said first and second narrow processing gaps from getting into said supply chamber and said reception cavity respectively from the outlet opening of said reception cavity through the said second narrow processing gap.
18. the system according to claim 16 is characterized in that, the said first narrow processing gap and the second narrow processing gap comprises the gas access that is used for said at least a first gaseous state thing and the said at least a second gaseous state thing respectively.
19. the system according to claim 17 is characterized in that, the said first narrow processing gap and the second narrow processing gap comprises the gas access that is used for said at least a first gaseous state thing and the said at least a second gaseous state thing respectively.
20. the system according to claim 17 is characterized in that, the roof separately in the said first narrow processing gap and the second narrow processing gap is parallel to diapire, and said diffusion obstacle section comprises and the parallel diffusion obstacle roof of diffusion obstacle diapire.
21. system according to claim 20; It is characterized in that the said roof separately and the height between the said diapire in the said first narrow processing gap and the second narrow processing gap are that said diffusion hinders the said diffusion obstacle roof of section and the twice at least of the height between the said diffusion obstacle diapire.
22. the system according to claim 14 is characterized in that, the roof in the said first narrow processing gap and the second narrow processing gap and the height between the diapire are in the scope of 0.5-10mm.
23. the system according to claim 22 is characterized in that, the width between the sidewall in the said first narrow processing gap is in the scope of 100-2000mm, and the width between the sidewall in the second narrow processing gap is in the scope of 100-2000mm.
24. one kind moves through volume forms diaphragm type IBIIIAVIA family solar absorber layer when rolling up rapid thermal treatment (RTP) chamber on the surface of said continuous flexible sheet-like workpiece method at the continuous flexible sheet-like workpiece; Wherein, said volume comprises to rolling up the rapid thermal treatment chamber: first processing section; Second processing section; And the diffusion that is arranged between said first processing section and said second processing section hinders section; Be provided with the gas access in the said diffusion obstacle section; Wherein, Said first processing section comprises first inlet, first outlet and first floss hole, and said second processing section comprises second inlet, second outlet and second floss hole, and said method comprises:
On the surface of said continuous flexible sheet-like workpiece, form precursor layer, said precursor layer comprises IB family material, and comprises at least a in IIIA family material and the VIA family material;
Be formed with the part of unwinding in advance on the feed rolls of the said continuous flexible sheet-like workpiece of precursor layer on it through feeding; The part of said continuous flexible sheet-like workpiece is moved in said first processing section through said first inlet, and move towards said first outlet;
Through getting into said diffusion obstacle section from said gas access and flow to inert gas flow that said first outlet and said second enters the mouth, the first gaseous state thing the processing section of winning be prevented from entering basically apply first Temperature Distribution when the second gaseous state thing in second processing section and second processing section is prevented from entering first processing section basically and utilize the said first gaseous state thing and in said first processing section, said precursor layer is handled setting up;
The said part that transmits said continuous flexible sheet-like workpiece makes it to hinder said second processing section motion of Duan Bingchao through said diffusion;
Through when continuing said inert gas flow, applying second Temperature Distribution and utilizing the said second gaseous state thing and in said second processing section, said precursor layer is handled; And
Pick up the processing section of said continuous flexible sheet-like workpiece and it is wound on from said second outlet of said second processing section and receive on the roller.
25. the method according to claim 24 is characterized in that, continuous flexible sheet-like workpiece IB family material is copper (Cu), and IIIA family material is at least a in indium (In) and the gallium (Ga), and VIA family material is selenium (Se).
26. method according to claim 25; It is characterized in that; Said first Temperature Distribution comprises near the roughly room temperature said first inlet and is changed to the distribution towards first temperature of first floss hole, and said second Temperature Distribution comprises near the distribution of roughly room temperature near second variations in temperature said second floss hole to said second outlet.
27. the method according to claim 24 is characterized in that, the group that said first gaseous state thing and the said second gaseous state thing are selected from the gas that comprises inert gas, comprises selenium and comprise the gas of sulphur.
28. method according to claim 24; It is characterized in that; Further comprise utilizing and set up first gas stream and utilize second gas that flows into said second processing section through said second outlet to set up second gas stream through first gas of said first processing section of the said first inlet inflow; Thereby prevent that the first gaseous state thing in first processing section from leaving first processing section through said first inlet; And feasible first emission gases by its generation is directed to first floss hole through first gas stream; And prevent that the second gaseous state thing in second processing section from leaving second processing section through said second outlet, and make second emission gases by its generation be directed to second floss hole through second gas stream.
29. the method according to claim 28 is characterized in that, the group that said first gas and said second gas are selected from the gas that comprises inert gas, comprises selenium and comprise the gas of sulphur.
30. the method according to claim 28 is characterized in that, the group that said first gas, second gas, the first gaseous state thing and the second gaseous state thing are selected from the gas that comprises inert gas, comprises selenium and comprise the gas of sulphur.
31. the method according to claim 30 is characterized in that, said first gas and said second gas are inert gases, and the said first gaseous state thing is the gas that comprises selenium, and the said second gaseous state thing is the gas that comprises sulphur.
32. the method according to claim 30 is characterized in that, said precursor layer comprises selenium (Se), and first gas, second gas and the first gaseous state thing are inert gases, and the second gaseous state thing is the gas that comprises sulphur.
33. the method according to claim 30 is characterized in that, said precursor layer comprises selenium (Se), and first gas, second gas and the first gaseous state thing are inert gases, and the second gaseous state thing is the gas that comprises selenium.
34. the method according to claim 30 is characterized in that, said precursor layer comprises selenium (Se), and first gas, second gas, the first gaseous state thing and the second gaseous state thing are inert gases.
35. one kind moves through volume forms diaphragm type IBIIIAVIA family solar absorber layer when rolling up rapid thermal treatment (RTP) chamber on the surface of said continuous flexible sheet-like workpiece method at the continuous flexible sheet-like workpiece; Wherein, Said volume comprises to rolling up the rapid thermal treatment chamber: the close clearance processing section; Said close clearance processing section comprises inlet, exports and is arranged on the discharge portion between said inlet and the said outlet, and said method comprises:
On the surface of said continuous flexible sheet-like workpiece, form precursor layer, said precursor layer comprises IB family material, and comprises at least a in IIIA family material and the VIA family material;
The part of the unwinding in advance on the feed rolls through the said continuous flexible sheet-like workpiece of feeding makes the part of said continuous flexible sheet-like workpiece move in the said close clearance processing section through said inlet, and moves towards said outlet;
Thereby through preventing that basically the gaseous state thing the said close clearance processing section from leaving said processing section and the said discharge portion that leads through said inlet and said outlet setting up second gas stream that gets into first gas stream of said close clearance processing section from said inlet and get into said close clearance processing section from said outlet; Apply first Temperature Distribution simultaneously, in said close clearance processing section, handle said precursor layer; And
Pick up the processing section of said continuous flexible sheet-like workpiece and it is wound on from the said outlet of said close clearance processing section and receive on the roller.
36. the method according to claim 35 is characterized in that, IB family material is copper (Cu), and IIIA family material is at least a in indium (In) and the gallium (Ga), and VIA family material is selenium (Se).
37. method according to claim 36; It is characterized in that; Said first Temperature Distribution comprises the distribution that is changed to the elevated temperature between said inlet and the said outlet near the roughly room temperature the entrance and exit of said close clearance processing section; And, the speed of said first gas stream and said second gas stream is selected, make to prevent that gaseous state thing in the said close clearance processing section is to said inlet and said outlet diffusion and be condensate on the said continuous flexible sheet-like workpiece.
38. the method according to claim 37 is characterized in that, said first gas and second gas are selected from the gas that comprises inert gas, comprises selenium and comprise the group of the gas of sulphur.
39. the method according to claim 37 is characterized in that, also comprising to said close clearance processing section provides processing gas.
40. the method according to claim 39 is characterized in that, said first gas and second gas are inert gases, and said processing gas is selected from the gas that comprises inert gas, comprises selenium and comprises the group of the gas of sulphur.
41. the method according to claim 40 is characterized in that, said precursor layer comprises selenium (Se), and first gas and second gas are inert gases, and said processing gas is selected from the gas that comprises inert gas, comprises selenium and comprises the group of the gas of sulphur.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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US86538506P | 2006-11-10 | 2006-11-10 | |
US60/865,385 | 2006-11-10 | ||
PCT/US2007/084432 WO2008085604A2 (en) | 2006-11-10 | 2007-11-12 | Reel-to-reel reaction of precursor film to form solar cell absorber |
Publications (2)
Publication Number | Publication Date |
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CN101578707A CN101578707A (en) | 2009-11-11 |
CN101578707B true CN101578707B (en) | 2012-08-22 |
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CN2007800464593A Expired - Fee Related CN101578707B (en) | 2006-11-10 | 2007-11-12 | Reel-to-reel reaction of precursor film to form solar cell absorber |
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Country | Link |
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EP (1) | EP2102898A4 (en) |
JP (1) | JP2010509779A (en) |
KR (1) | KR20090110293A (en) |
CN (1) | CN101578707B (en) |
TW (1) | TW200832726A (en) |
WO (1) | WO2008085604A2 (en) |
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TWI424073B (en) * | 2007-09-11 | 2014-01-21 | Centrotherm Photovoltaics Ag | Method and apparatus for thermally converting metallic precursor layers into semiconductor layers, and also solar module |
US8323408B2 (en) | 2007-12-10 | 2012-12-04 | Solopower, Inc. | Methods and apparatus to provide group VIA materials to reactors for group IBIIIAVIA film formation |
US8163090B2 (en) * | 2007-12-10 | 2012-04-24 | Solopower, Inc. | Methods structures and apparatus to provide group VIA and IA materials for solar cell absorber formation |
KR20110097908A (en) * | 2008-11-28 | 2011-08-31 | 볼커 프로브스트 | Method for producing semiconductor layers and coated substrates treated with elemental selenium and/or sulfur, in particular flat substrates |
DE102009009022A1 (en) * | 2009-02-16 | 2010-08-26 | Centrotherm Photovoltaics Ag | Method and device for coating flat substrates with chalcogens |
TWI509107B (en) * | 2009-03-06 | 2015-11-21 | Centrotherm Photovoltaics Ag | Verfahren und vorrichtung zur thermischen umsetzung metallischer precusorschichten in halbleitende schichten mit chalkogenquelle |
DE102009011496A1 (en) * | 2009-03-06 | 2010-09-16 | Centrotherm Photovoltaics Ag | Process and device for the thermal conversion of metallic precursor layers into semiconducting layers with chalcogen recovery |
DE102009049570B3 (en) * | 2009-10-15 | 2011-02-17 | Fhr Anlagenbau Gmbh | Arrangement for gas separation and its use |
TWI398013B (en) * | 2009-12-18 | 2013-06-01 | Jenn Feng New Energy Co Ltd | Method and system for forming non-vacuum copper indium gallium sulphide selenium absorption layer and cadmium sulfide buffer layer |
WO2011132915A2 (en) * | 2010-04-19 | 2011-10-27 | 한국생산기술연구원 | Method for manufacturing solar cell |
CN103403851A (en) * | 2011-03-10 | 2013-11-20 | 法国圣戈班玻璃厂 | Method for producing the pentanary compound semiconductor CZTSSe, and thin-film solar cell |
JP2012222157A (en) * | 2011-04-08 | 2012-11-12 | Hitachi Kokusai Electric Inc | Substrate processing apparatus and method of manufacturing solar cell |
EP2834853A4 (en) * | 2012-02-29 | 2015-12-09 | Alliance Sustainable Energy | SYSTEMS AND METHODS FOR FORMING SOLAR CELLS WITH CuInSe2 AND Cu(In,Ga)Se2 FILMS |
CN103361603A (en) * | 2012-03-29 | 2013-10-23 | 常熟卓辉光电科技有限公司 | Vacuum evaporation equipment of semiconductor film material and preparation method of OLED (Organic Light Emitting Diode) conductive layer |
DE102012205378A1 (en) * | 2012-04-02 | 2013-10-02 | Robert Bosch Gmbh | Process for the production of thin-film solar modules and thin-film solar modules obtainable by this process |
KR101461315B1 (en) * | 2012-06-19 | 2014-11-12 | 가부시키가이샤 스크린 홀딩스 | Heat treatment apparatus and heat treatment method |
CN104937706B (en) * | 2012-07-09 | 2019-02-26 | 蚌埠玻璃工业设计研究院 | Device and method for processing a substrate |
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- 2007-11-12 EP EP07872342A patent/EP2102898A4/en not_active Withdrawn
- 2007-11-12 CN CN2007800464593A patent/CN101578707B/en not_active Expired - Fee Related
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- 2007-11-12 JP JP2009536531A patent/JP2010509779A/en active Pending
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Also Published As
Publication number | Publication date |
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EP2102898A4 (en) | 2011-06-29 |
WO2008085604B1 (en) | 2008-12-24 |
TW200832726A (en) | 2008-08-01 |
JP2010509779A (en) | 2010-03-25 |
EP2102898A2 (en) | 2009-09-23 |
CN101578707A (en) | 2009-11-11 |
WO2008085604A3 (en) | 2008-10-16 |
WO2008085604A2 (en) | 2008-07-17 |
KR20090110293A (en) | 2009-10-21 |
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